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Article: Indium tribromide-promoted arene-terminated epoxy olefin cyclization

TitleIndium tribromide-promoted arene-terminated epoxy olefin cyclization
Authors
Zhao, JFZhao, YJLoh, TP
Issue Date2008
PublisherRoyal Society of Chemistry. The Journal's web site is located at http://www.rsc.org/Publishing/Journals/cc/index.asp
Citation
Chemical Communications, 2008 n. 11, p. 1353-1355 How to Cite?
DOI: http://dx.doi.org/10.1039/b718337b
AbstractAn arene-terminated epoxy olefin cyclization was promoted by a water-tolerant Lewis acid to give tri- and tetracyclic 3β-hydroxy terpenoids and steroid derivatives in 57 and 37% yields, respectively, per new formed ring up to 75%. © The Royal Society of Chemistry.
Persistent Identifierhttp://hdl.handle.net/10722/182334
ISSN
1359-7345
2023 Impact Factor: 4.3
2023 SCImago Journal Rankings: 1.133
ISI Accession Number ID
WOS:000254352900027
References
References in Scopus

 

DC FieldValueLanguage
dc.contributor.authorZhao, JFen_US
dc.contributor.authorZhao, YJen_US
dc.contributor.authorLoh, TPen_US
dc.date.accessioned2013-04-23T08:18:58Z-
dc.date.available2013-04-23T08:18:58Z-
dc.date.issued2008en_US
dc.identifier.citationChemical Communications, 2008 n. 11, p. 1353-1355en_US
dc.identifier.issn1359-7345en_US
dc.identifier.urihttp://hdl.handle.net/10722/182334-
dc.description.abstractAn arene-terminated epoxy olefin cyclization was promoted by a water-tolerant Lewis acid to give tri- and tetracyclic 3β-hydroxy terpenoids and steroid derivatives in 57 and 37% yields, respectively, per new formed ring up to 75%. © The Royal Society of Chemistry.en_US
dc.languageengen_US
dc.publisherRoyal Society of Chemistry. The Journal's web site is located at http://www.rsc.org/Publishing/Journals/cc/index.aspen_US
dc.relation.ispartofChemical Communicationsen_US
dc.subject.meshAlkenes - Chemistryen_US
dc.subject.meshCrystallography, X-Rayen_US
dc.subject.meshCyclizationen_US
dc.subject.meshEpoxy Compounds - Chemical Synthesisen_US
dc.subject.meshIndicators And Reagentsen_US
dc.subject.meshIndium - Chemistryen_US
dc.subject.meshModels, Molecularen_US
dc.subject.meshMolecular Conformationen_US
dc.subject.meshSolventsen_US
dc.subject.meshSteroids - Chemical Synthesisen_US
dc.subject.meshTerpenes - Chemical Synthesisen_US
dc.titleIndium tribromide-promoted arene-terminated epoxy olefin cyclizationen_US
dc.typeArticleen_US
dc.identifier.emailZhao, JF: zhao0065@e.ntu.edu.sgen_US
dc.identifier.authorityZhao, JF=rp01745en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1039/b718337ben_US
dc.identifier.pmid18389131-
dc.identifier.scopuseid_2-s2.0-41749124571en_US
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-41749124571&selection=ref&src=s&origin=recordpageen_US
dc.identifier.issue11en_US
dc.identifier.spage1353en_US
dc.identifier.epage1355en_US
dc.identifier.isiWOS:000254352900027-
dc.publisher.placeUnited Kingdomen_US
dc.identifier.scopusauthoridZhao, JF=8393022100en_US
dc.identifier.scopusauthoridZhao, YJ=41862978100en_US
dc.identifier.scopusauthoridLoh, TP=35234192600en_US
dc.identifier.issnl1359-7345-

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